Angelman Announcements – 1 – 5 November 2012

Lancashire Evening Post
Ralph, 11, who goes to a special school in Bamber Bridge, was diagnosed with a rare genetic condition called Angelman Syndrome when he was 12 months old
Fundraiser Nov 10
By on Sat, Oct 27, 2012 Patrick Gonzales has spent many years watching his 12-year-old boys sit on the sidelines while his other four children play.
She has Angelman Syndrome, which keeps her in a wheelchair, but not walking hasn’t slowed her down. Her passion for being in the water has her using her
Blog UPDATES
Stop Seizures Now: A Nickel Spinning at the Restaurant  stopseizuresnow.blogspot.com
http://stopseizuresnow.blogspot.com/2012/11/three-years-since-death-of-my-boy.htmlTo any groups working for a cure for Angelman Syndrome, never ever give up. Keep doing exactly what you are doing. Much love to families who have been down a similar road.
Stop Seizures Now: Three Years Since the Death of my Boy

finnsfather.com

Occasionally, I take things for granted. So, occasionally, I need to be forced out of my comfort zone so that I might remember to be thankful for the things I have. Last night was one of those times when I was kicked far outside of my comfort zone. And it reminded me just how thankful I should be…
Brady’s Blog Update –
NEW YOUTUBE CHANNELS
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About humphriesnz

Live in Christchurch New Zealand with my family, Catholic, interested in music historic Fiction, Angelman Syndrome Awareness
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